Janice Smith - Coordinator Resume Simple
SUMMARY
A highly motivated, detail-oriented, and results-driven professional with over 10 years of experience in the medical field. I am a self-starter, able to work well independently and as a team member.
SKILLS
  • mri, management, ups, radiology, spreadsheets, patient, marketing, nuclear medicine, x ray, ct, excel spreadsheets, excel, imaging
  • analysis, phlebotomy, outlook, hippa, iv, database, nutrition, vital signs, research, clinical
WORK EXPERIENCES
  • 2017-12-252017-12-25

    Coordinator

    Parkway School District

    • Ensure that all patient information is complete and accurate, and the management is being sent to the provider. Maintain a spreadsheet of the patients.
    • Received training for the CT department and the x-ray department. This position was a full time position.
    • Develop and maintain relationships with physicians, nurses, and other staff members to facilitate the use of the practice.
    • Worked with the Director of the development of the office of the training of the CT department. The MRI Technologist, the nuclear Medicine Technologist, and the nuclear Medicine technologists.
    • Manage and oversee all aspects of radiology and lab work. Coordinate with outside vendors and outside vendors. Assist in the development of new and existing policies.
    • Responsible for the development of Excel spreadsheet and the creation of a comprehensive training manual. Created and maintained a web-based database.
  • 2017-12-252017-12-25

    Clinical Research Coordinator

    Deaconess Hospital

    • Conducted clinical assessments, vital signs, EKG, and collection of blood samples. Prepared and shipped blood samples.
    • Ensured that all study related documentation is completed in accordance with the protocol, including the consenting process, the study protocol, and the IRB.
    • Performed study related tasks such as clinical documentation, vital signs, and informed consent process. Assisted with the preparation of IRB submissions.
    • Developed and maintained source documentation for all study activities including data collection, clinical trials, and informed consent forms.
    • Collection of source documents for accuracy and completeness. Provided data review to the clinical study coordinators. Assisted with the preparation of study reports.
    • Developed and maintained source documentation for all study activities including data collection, clinical trials, and informed consent forms.